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rs180177034

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177034(C;C)
Make rs180177034(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position140801536
GeneBRAF
is asnp
is mentioned by
dbSNPrs180177034
ebirs180177034
HLIrs180177034
Exacrs180177034
Varsomers180177034
Maprs180177034
PheGenIrs180177034
hapmaprs180177034
1000 genomesrs180177034
hgdprs180177034
ensemblrs180177034
gopubmedrs180177034
geneviewrs180177034
scholarrs180177034
googlers180177034
pharmgkbrs180177034
gwascentralrs180177034
openSNPrs180177034
23andMers180177034
23andMe allrs180177034
SNP Nexus

SNPshotrs180177034
SNPdbers180177034
MSV3drs180177034
GWAS Ctlgrs180177034
Max Magnitude0
ClinVar
Risk rs180177034(C;C)
Alt rs180177034(C;C)
Reference rs180177034(G;G)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome 1 Rasopathy Cardiofaciocutaneous syndrome not provided
Variation info
Gene BRAF
CLNDBN Cardiofaciocutaneous syndrome 1 Rasopathy Cardiofaciocutaneous syndrome not provided
Reversed 1
HGVS NC_000007.13:g.140501336C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014998.26, RCV000033285.6, RCV000208416.1, RCV000235118.1,